A citation-based method for searching scientific literature

Xizhi Luo, Fei Qin, Guoshuai Cai, Feifei Xiao. Bioinformatics 2021
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Integrating common and rare genetic variation in diverse human populations.
David M Altshuler, Richard A Gibbs, Leena Peltonen, David M Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil Dermitzakis, Stephen F Schaffner, Fuli Yu, Leena Peltonen,[...]. Nature 2010
100

CoNVEX: copy number variation estimation in exome sequencing data using HMM.
Kaushalya C Amarasinghe, Jason Li, Saman K Halgamuge. BMC Bioinformatics 2013
39
100

Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2.
Romina D'Aurizio, Tommaso Pippucci, Lorenzo Tattini, Betti Giusti, Marco Pellegrini, Alberto Magi. Nucleic Acids Res 2016
44
100

The clinical significance of small copy number variants in neurodevelopmental disorders.
Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger,[...]. J Med Genet 2014
55
100

Human genome sequencing in health and disease.
Claudia Gonzaga-Jauregui, James R Lupski, Richard A Gibbs. Annu Rev Med 2012
255
100

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Menachem Fromer, Jennifer L Moran, Kimberly Chambert, Eric Banks, Sarah E Bergen, Douglas M Ruderfer, Robert E Handsaker, Steven A McCarroll, Michael C O'Donovan, Michael J Owen,[...]. Am J Hum Genet 2012
331
100

CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data.
Qunyuan Zhang, Li Ding, David E Larson, Daniel C Koboldt, Michael D McLellan, Ken Chen, Xiaoqi Shi, Aldi Kraja, Elaine R Mardis, Richard K Wilson,[...]. Bioinformatics 2010
42
100

3
100


Circular binary segmentation for the analysis of array-based DNA copy number data.
Adam B Olshen, E S Venkatraman, Robert Lucito, Michael Wigler. Biostatistics 2004
100


Copy number variation distribution in six monozygotic twin pairs discordant for schizophrenia.
Christina A Castellani, Zain Awamleh, Melkaye G Melka, Richard L O'Reilly, Shiva M Singh. Twin Res Hum Genet 2014
25
100

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
100

PennCNV in whole-genome sequencing data.
Leandro de Araújo Lima, Kai Wang. BMC Bioinformatics 2017
7
100

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
95
100

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.
Fatima Zare, Michelle Dow, Nicholas Monteleone, Abdelrahman Hosny, Sheida Nabavi. BMC Bioinformatics 2017
57
100

Multiple Change-Point Detection via a Screening and Ranking Algorithm.
Ning Hao, Yue Selena Niu, Heping Zhang. Stat Sin 2013
7
100

CODEX: a normalization and copy number variation detection method for whole exome sequencing.
Yuchao Jiang, Derek A Oldridge, Sharon J Diskin, Nancy R Zhang. Nucleic Acids Res 2015
73
100

A shifting level model algorithm that identifies aberrations in array-CGH data.
Alberto Magi, Matteo Benelli, Giuseppina Marseglia, Genni Nannetti, Maria Rosaria Scordo, Francesca Torricelli. Biostatistics 2010
19
100

An accurate and powerful method for copy number variation detection.
Feifei Xiao, Xizhi Luo, Ning Hao, Yue S Niu, Xiangjun Xiao, Guoshuai Cai, Christopher I Amos, Heping Zhang. Bioinformatics 2019
2
100

modSaRa: a computationally efficient R package for CNV identification.
Feifei Xiao, Yue Niu, Ning Hao, Yanxun Xu, Zhilin Jin, Heping Zhang. Bioinformatics 2017
3
100

EXCAVATOR: detecting copy number variants from whole-exome sequencing data.
Alberto Magi, Lorenzo Tattini, Ingrid Cifola, Romina D'Aurizio, Matteo Benelli, Eleonora Mangano, Cristina Battaglia, Elena Bonora, Ants Kurg, Marco Seri,[...]. Genome Biol 2013
147
100


Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.
Jarupon Fah Sathirapongsasuti, Hane Lee, Basil A J Horst, Georg Brunner, Alistair J Cochran, Scott Binder, John Quackenbush, Stanley F Nelson. Bioinformatics 2011
266
100

Identification of germline genomic copy number variation in familial pancreatic cancer.
Wigdan Al-Sukhni, Sarah Joe, Anath C Lionel, Nora Zwingerman, George Zogopoulos, Christian R Marshall, Ayelet Borgida, Spring Holter, Aaron Gropper, Sara Moore,[...]. Hum Genet 2012
18
100

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.
Alberto Magi, Matteo Benelli, Seungtai Yoon, Franco Roviello, Francesca Torricelli. Nucleic Acids Res 2011
50
100

CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing.
Yuchao Jiang, Rujin Wang, Eugene Urrutia, Ioannis N Anastopoulos, Katherine L Nathanson, Nancy R Zhang. Genome Biol 2018
17
100

A functional copy-number variation in MAPKAPK2 predicts risk and prognosis of lung cancer.
Bin Liu, Lei Yang, Binfang Huang, Mei Cheng, Hui Wang, Yinyan Li, Dongsheng Huang, Jian Zheng, Qingchu Li, Xin Zhang,[...]. Am J Hum Genet 2012
50
100

A very fast and accurate method for calling aberrations in array-CGH data.
Matteo Benelli, Giuseppina Marseglia, Genni Nannetti, Roberta Paravidino, Federico Zara, Franca Dagna Bricarelli, Francesca Torricelli, Alberto Magi. Biostatistics 2010
12
100

Copy number variation detection and genotyping from exome sequence data.
Niklas Krumm, Peter H Sudmant, Arthur Ko, Brian J O'Roak, Maika Malig, Bradley P Coe, Aaron R Quinlan, Deborah A Nickerson, Evan E Eichler. Genome Res 2012
359
100

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
100

Integrated detection and population-genetic analysis of SNPs and copy number variation.
Steven A McCarroll, Finny G Kuruvilla, Joshua M Korn, Simon Cawley, James Nemesh, Alec Wysoker, Michael H Shapero, Paul I W de Bakker, Julian B Maller, Andrew Kirby,[...]. Nat Genet 2008
687
100

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
100


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.